dc.contributor | Mostardeiro, Marco Aurelio | |
dc.contributor | http://lattes.cnpq.br/6195396264565980 | |
dc.contributor | Dalcol, Ionara Irion | |
dc.contributor | http://lattes.cnpq.br/9769548819312192 | |
dc.contributor | Ilha, Vinicius | |
dc.contributor | http://lattes.cnpq.br/3882671719676564 | |
dc.creator | Reis, Frederico Luiz | |
dc.date.accessioned | 2018-11-27T10:41:03Z | |
dc.date.accessioned | 2019-05-24T20:31:13Z | |
dc.date.available | 2018-11-27T10:41:03Z | |
dc.date.available | 2019-05-24T20:31:13Z | |
dc.date.created | 2018-11-27T10:41:03Z | |
dc.date.issued | 2018-07-17 | |
dc.identifier | http://repositorio.ufsm.br/handle/1/14945 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/2841673 | |
dc.description.abstract | The phytochemical investigation of hexane and methanolic crude extracts and their fractions from the
bark of the stem of Tabernaemontana catharinensis (Apocynaceae, commonly known as cobrina) led
to the isolation of nine monoterpene indole alkaloids, voachalotin, affinisine, 16-epiaffinisin,
voacangin, voacristin, vinpocetine, voacangine hydroxylindolenine, 12-methoxy-N4-methyl
voachalotine and 12-methoxy-N4-methyl-5-epiquachalotine. The alkaloid vinpocetine and 12-
methoxy-N4-methyl-5-epi voachalotin are isolated for the first time in the family Apocynaceae. A Nmethyl
affinisine derivative was obtained through an affinisin methylation reaction. The extracts,
fractions and isolated compounds showed antibacterial activity (Gram-positive and Gram-negative)
and effective antifungal, against the tested strains. The inhibitory potential of the pairs of
diastereoisomers, corinantean skeleton, affinisine, 16-epiaffinisina and 12-methoxy-N4-methyl-5-
epivoachalotine, 12-methoxy-N4-methyl voachalotine presented MIC values (1.56 μg.mL -1) lower
than the fluconazole standard (MIC 3.12 μg.mL-1) compared to fungal strains. The methylation of the
affinisine compound potentiated the inhibition against some microorganisms. The ibogan skeletal
alkaloids, Voacangina, and Voacristina presented better inhibitory potentials against bacteria,
presenting MIC of 3.12; 12.5 and 25 μg.mL -1 against the microorganisms Pseudomonas aeroginosa,
Bacillus cereus and Salmonella typhimurium, respectively, being equal to or close to the
chloramphenicol standard. The importance of stereochemistry in relation to the effectiveness of the
MIC, which is visible in the activities presented in this paper. Thus, the phytochemical study and the
pharmacological activities of the identified compounds of the stem bark of T.catharinensis broaden the
knowledge alluding to chemotaxonomy, as well as justifying its antifungal use in folk medicine. | |
dc.publisher | Universidade Federal de Santa Maria | |
dc.publisher | Brasil | |
dc.publisher | Química | |
dc.publisher | UFSM | |
dc.publisher | Programa de Pós-Graduação em Química | |
dc.publisher | Centro de Ciências Naturais e Exatas | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
dc.subject | Tabernaemontana catharinensis | |
dc.subject | Alcaloide indólico | |
dc.subject | Vinpocetina | |
dc.subject | Atividade antimicrobiana | |
dc.subject | Indole alkaloid | |
dc.subject | Vinpocetine | |
dc.subject | Antimicrobian activity | |
dc.title | Investigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas | |
dc.type | Tesis | |